Evaluate the Continued Safety and Performance of the Foot and Ankle Products

Summary

The objective of the registry is to evaluate the continued safety and performance of Arthrex foot and ankle products, including the ProStop® implant for hyperpronated foot; Bio-Compression Screw for reconstruction surgeries of the foot; TRIM-IT Drill Pin® system and/or TRIM-IT Spin Pin™ system for fixation of fractures and fusion (bunionectomy osteotomies) of the foot/ankle; Headless Compression Screws and Compression FT Screws for fixation of small bone fragments of the foot/ankle; DynaNite® nitinol staple for midfoot and hindfoot arthrodeses or osteotomies, first metatarsophalangeal…

Shortened from the sponsor's brief summary. View official record on ClinicalTrials.gov

Conditions studied

• Hyperpronated Foot
• Reconstruction Surgeries of the Foot
• Fixation of Fractures and Fusion (Bunionectomy Osteotomies) of the Foot/Ankle
• Fixation of Small Bone Fragments of the Foot/Ankle
• Lisfranc Arthrodesis
• Mono or Bi-cortical Osteotomies in the Forefoot
• First Metatarsophalangeal Arthrodesis
• Akin Osteotomy
• Midfoot and Hindfoot Arthrodeses or Osteotomies
• Fixation of Osteotomies for Hallux Valgus Treatment (Scarf and Chevron)
• Arthrodesis of the Metatarsocuneiform Joint to Reposition and Stabilize Metatarsus Primus Varus
• Osteotomy Fixation of Hallux Valgus Repair (Such as Scarf and Chevron Etc.)
• Medial Ankle Stabilization
• Tibiotalocalcaneal Arthrodesis

Eligibility basics and study details

Study type

Observational

Phase

Not applicable

Ages

2 years and older

Sex

All

Healthy volunteers

Accepted

Sponsor

Arthrex, Inc.

Last updated on ClinicalTrials.gov

February 11, 2026

These are the basic criteria only. The full inclusion and exclusion criteria are on the official record, and the study team decides who can take part.

US recruiting sites